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Vβ17a+ CD8+ T细胞杂交体的反应性。使用新的CD8+ T细胞融合伴侣进行分析。

Reactivity of V beta 17a+ CD8+ T cell hybrids. Analysis using a new CD8+ T cell fusion partner.

作者信息

Burgert H G, White J, Weltzien H U, Marrack P, Kappler J W

机构信息

Howard Hughes Medical Institute, Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.

出版信息

J Exp Med. 1989 Dec 1;170(6):1887-904. doi: 10.1084/jem.170.6.1887.

Abstract

Tolerance to IE molecules leads to deletion of V beta 17a-bearing T cells. Both, the CD4+ as well as the CD8+ T cell subsets are affected. A large percentage of CD4+ V beta 17a+ T cell hybrids recognize IE molecules. We now have investigated the reactivity for IE antigens of CD8+ V beta 17a+ T cell hybrids. Using a transfection approach, we have introduced the murine CD8 molecule into different V beta 17a+ T cell hybrids. Furthermore, the CD8 cDNA was transfected into the BW5147 alpha-beta- fusion partner. This allowed us to generate a large number of V beta 17a+ T cell hybrids by fusion with the appropriate T cells. Only 6% of T cell hybrids were stimulated to produce IL-2 upon incubation with IE+ cells. However, in those, the CD8 molecule seemed not to contribute to the IE reactivity of the hybrid, since mAbs against the CD8 molecule failed to inhibit their reactivity. This low percentage of V beta 17a+ CD8+ IE-reactive T cell hybrids contrasts with the strong reduction of CD8+ V beta 17a+ T cells in IE+ mice, strongly suggesting that elimination of such cells in the thymus occurs when they are coexpressing CD4 and CD8. This view was confirmed by the occasional expression of CD4 in some hybrids in which case IE reactivity was detected. Furthermore, we demonstrated the functional integrity of the introduced CD8 molecule by: (a) reconstitution of the IL-2 response in a class I-restricted TNP-specific T cell hybrid; and (b) by generation of alloreactive class I-restricted T cell hybrids using the new CD8+ fusion cell line. This CD8+ fusion partner, BWLyt2-4, should prove useful to study antigen processing and antigen presentation requirements of class I-restricted T cells.

摘要

对IE分子的耐受性导致携带Vβ17a的T细胞缺失。CD4⁺和CD8⁺T细胞亚群均受影响。很大比例的CD4⁺Vβ17a⁺T细胞杂交瘤识别IE分子。我们现在研究了CD8⁺Vβ17a⁺T细胞杂交瘤对IE抗原的反应性。采用转染方法,我们将小鼠CD8分子导入不同的Vβ17a⁺T细胞杂交瘤中。此外,将CD8 cDNA转染到BW5147α-β融合伙伴中。这使我们能够通过与合适的T细胞融合产生大量的Vβ17a⁺T细胞杂交瘤。与IE⁺细胞孵育后,只有6%的T细胞杂交瘤被刺激产生IL-2。然而,在这些杂交瘤中,CD8分子似乎对杂交瘤的IE反应性没有贡献,因为针对CD8分子的单克隆抗体未能抑制其反应性。Vβ17a⁺CD8⁺IE反应性T细胞杂交瘤的这一低比例与IE⁺小鼠中CD8⁺Vβ17a⁺T细胞的强烈减少形成对比,强烈表明此类细胞在胸腺中共同表达CD4和CD8时会被清除。在一些检测到IE反应性的杂交瘤中偶尔表达CD4,这证实了这一观点。此外,我们通过以下方式证明了导入的CD8分子的功能完整性:(a)在I类限制性TNP特异性T细胞杂交瘤中重建IL-2反应;(b)使用新的CD8⁺融合细胞系产生同种异体反应性I类限制性T细胞杂交瘤。这种CD8⁺融合伙伴BWLyt2-4应该对研究I类限制性T细胞的抗原加工和抗原呈递要求有用。

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